68725-14-4CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[O]S(=O)(=O)C(F)(F)FLIQOILBASIAIQC-UHFFFAOYSA-M68725-14-4White to light beige crystals and chunks
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Danger
H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]
P260, P264, P264+P265, P270, P273, P280, P301+P316, P302+P352, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P391, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
용도Tri-n-butyltin Trifluoromethanesulfonate is a powerful stannylating reagent. It readily stannylates vinylcuprates and vinylaluminum compounds; catalyzes hydrostannation of aldehydes and ketones by tin hydrides.
Tribuyltin trifluoromethanesulfonate is prepared from Bis(tri-n-butyltin) Oxide and either Trifluoromethanesulfonic Acid (with subsequent removal of water) or Trifluoromethanesulfonic Anhydride, as in eq 1.The following procedure is quite convenient: freshly distilled trifluoromethanesulfonic anhydride is caused to react with an equal molar amount of tributyltin oxide cooled at 20 °C under nitrogen. When the exothermic reaction completely subsides, the flask is set up for a short-path distillation and the resulting red oil is distilled at about 0.1 mmHg. The distillate is collected without cooling to prevent crystallization of the product in the condenser. Alternatively, this reagent can be prepared in situ by the action of trifluoromethanesulfonic acid on Tri-n-butylstannane in benzene or dichloroethane.
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